52763-21-0

  • Product Name:Ethyl N-benzyl-3-oxo-4-piperidine-carboxylate hydrochloride
  • Molecular Formula:C15H20ClNO3
  • Purity:99%
  • Molecular Weight:297.782
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Product Details;

CasNo: 52763-21-0

Molecular Formula: C15H20ClNO3

Appearance: white to brown crystalline powder

Factory Sells Best Quality Ethyl N-benzyl-3-oxo-4-piperidine-carboxylate hydrochloride 52763-21-0 with USP

  • Molecular Formula:C15H20ClNO3
  • Molecular Weight:297.782
  • Appearance/Colour:white to brown crystalline powder 
  • Vapor Pressure:1.26E-05mmHg at 25°C 
  • Melting Point:162 °C (dec.)(lit.) 
  • Boiling Point:368.6 °C at 760 mmHg 
  • Flash Point:176.7 °C 
  • PSA:46.61000 
  • Density:1.154 g/cm3 
  • LogP:2.38060 

Ethyl N-benzyl-3-oxo-4-piperidine-carboxylate hydrochloride(Cas 52763-21-0) Usage

InChI:InChI=1/C15H19NO3/c1-2-19-15(18)13-8-9-16(11-14(13)17)10-12-6-4-3-5-7-12/h3-7,13H,2,8-11H2,1H3/p+1/t13-/m1/s1

52763-21-0 Relevant articles

Preparation method of N-benzyl-3-oxopiperidine-4-carboxylic acid ethyl ester hydrochloride

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Paragraph 0006; 0018; 0022-0026; 0030-0034; 0038-0041, (2020/02/10)

The invention provides a preparation met...

Process development and scale-up of a selective α1- adrenoceptor antagonist

Connolly, Terrence J.,Matchett, Michael,Sarma, Keshab

, p. 80 - 87 (2012/12/24)

A synthetic route to a potent and select...

Efficient enantioselective synthesis of the NMDA 2B receptor antagonist Ro 67-8867

Scalone, Michelangelo,Waldmeier, Pius

, p. 418 - 425 (2013/09/06)

An efficient, enantioselective, and scal...

Process for the preparation of ethanesul fonyl-piperidine derivatives

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, (2008/06/13)

The present invention relates to a new p...

52763-21-0 Process route

4-[benzyl(ethoxycarbonylmethyl)amino]butyric acid ethyl ester
63876-32-4

4-[benzyl(ethoxycarbonylmethyl)amino]butyric acid ethyl ester

ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride
52763-21-0

ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride

Conditions
Conditions Yield
4-[benzyl(ethoxycarbonylmethyl)amino]butyric acid ethyl ester; With sodium ethanolate; In toluene; at 20 - 85 ℃; for 3.5h; Large scale;
With hydrogenchloride; In water; toluene; Large scale;
94%
4-[benzyl(ethoxycarbonylmethyl)amino]butyric acid ethyl ester; With sodium methylate; In ethyl acetate; for 4h; Reflux; Large scale;
With water; sodium hydroxide; pH=7 - 8; Large scale;
With hydrogenchloride; pH=1 - 2; Reagent/catalyst; Solvent; Large scale;
8.6 kg
ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate
39514-19-7

ethyl 1-benzyl-3-oxo-4-piperidinecarboxylate

ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride
52763-21-0

ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride

Conditions
Conditions Yield
With hydrogenchloride; In ethanol; at 22 ℃; for 0.5h; Inert atmosphere; Large scale;
76.8%

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